Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PRE-CUT TRACHEOSTOMY DRESSING STERILE, DISPOSABLE

K-Number: K920282 · 1992-05-29

ApplicantTrinity Laboratories, Inc.
Decision Date1992-05-29
Product CodeNAB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PRE-CUT TRACHEOSTOMY DRESSING STERILE, DISPOSABLE is the device name listed in this FDA 510(k) record. The listed applicant is Trinity Laboratories, Inc.. It received FDA 510(k) clearance on 1992-05-29 under 510(k) number K920282. The device is classified under product code NAB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRE-CUT TRACHEOSTOMY DRESSING STERILE, DISPOSABLE?

PRE-CUT TRACHEOSTOMY DRESSING STERILE, DISPOSABLE is a medical device that received FDA 510(k) clearance on 1992-05-29. The listed applicant is Trinity Laboratories, Inc.. The 510(k) number is K920282.

When did PRE-CUT TRACHEOSTOMY DRESSING STERILE, DISPOSABLE receive FDA 510(k) clearance?

PRE-CUT TRACHEOSTOMY DRESSING STERILE, DISPOSABLE received FDA 510(k) clearance on 1992-05-29, under 510(k) number K920282.

Who is the listed applicant for PRE-CUT TRACHEOSTOMY DRESSING STERILE, DISPOSABLE?

The FDA 510(k) record lists Trinity Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRE-CUT TRACHEOSTOMY DRESSING STERILE, DISPOSABLE?

The FDA product code for PRE-CUT TRACHEOSTOMY DRESSING STERILE, DISPOSABLE is NAB.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Trinity Laboratories, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K981441HEART CATH TRAY, STERILE, DISPOSABLEK974238DENTAL TRAY, STERILE, DISPOSABLEK974286CIRCUMCISION TRAY, CAT. NO. 70340K972160CRP-LEX SYSTEM: C-REACTIVE PROTEIN ANTIGEN DETECTION IN SERUM: SLIDE AGGLUTNATION LATEX TESTK970722EYE TRAYK965201O.R. SCRUB PREP TRAY, STERILE, DISPOSABLE

View all 44 devices →

Related Devices (Code: NAB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K946015IVALON EXTERNAL SPONGEIvalonK940755ISOLYER (4X4, 8PLY)Isolyer Co.K931610OMNISORB II, NONWOVEN SPONGE, STERILE AND NONOmni Mfg., Inc.K925590MULTI-TRAUMA DRESSINGGam Industries, Inc.K926072K-BAND AND K-CREPEParema , Ltd.K915591STERILE GAUZE PADSEagle Medical, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑